Group Quality Management System Manager
il y a 4 semaines
We are EssilorLuxottica, a global leader in the design, manufacture and distribution of ophthalmic lenses, frames and sunglasses. The Company brings together the complementary expertise of two industry pioneers, one in advanced lens technologies and the other in the craftsmanship of iconic eyewear, to create a vertically integrated business that is uniquely positioned to address the world's evolving vision needs and the global demand of a growing eyewear industry.
With over 180,000 dedicated employees in 150 countries driving our iconic brands, our people are creative, entrepreneurial and celebrated for their unique perspectives and individuality. Committed to vision, we enable people to "see more and be more" thanks to our innovative designs and lens technologies, exceptional quality and cutting-edge processing methods. Every day we impact the lives of millions by changing the way people see the world.
Job Overview:
- Develop and maintain the Group Ophthalmic Lens Quality System, ensuring compliance with all applicable medical device regulations, standards, and best practices.
- Support the quality certification process of Legal Manufacturers and Manufacturing sites from a global QMS perspective.
- Design and implement a worldwide network to maintain and improve the Group QMS.
- Contribute to the qualification of Internal Auditors and support external inspections.
- Deploy and maintain quality documentation systems within the group.
Key Responsibilities:
- Shape and design the Group Ophthalmic Lens Quality System.
- Maintain compliance with external regulatory evolutions and internal business needs.
- Support quality certification processes.
- Develop and manage a worldwide network.
- Contribute to the qualification of Internal Auditors.
- Support external inspections.
- Deploy and maintain quality documentation systems.
Requirements:
- Holds a diploma in Engineering, Biology, Pharmacy, or Quality.
- Experience in Quality system management or design of new systems in medical device fields.
- Previous exposure to a multinational/global scope and good knowledge of regulations ISO 13 485, MDR, 21 CFR Part 820(FDA).
- Excellent technical writing skills in English, with French and/or Italian as a plus.
- Initiative and autonomy in a cross-functional position.
- Self-development capacity.
- Communication and influence skills at multiple levels.
- Extended experience with Quality.
- Transversal network management and Team Building.
- Capacity to transfer knowledge.
- Good interpersonal skills and business focus.
- Knowledge of the ophthalmic industry is a plus.
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